Canonical Allele Identifier: CA57289630

Gene: LRP1B

Linked Data

• dbSNP Id: rs185673864
• gnomAD v3: 2-141038111-G-T
• gnomAD v4: 2-141038111-G-T
• MyVariant Identifiers: chr2:g.141795680G>T (hg19) ; chr2:g.141038111G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.141038111G>T , CM000664.2:g.141038111G>T	GRCh38
NC_000002.11:g.141795680G>T , CM000664.1:g.141795680G>T	GRCh37
NC_000002.10:g.141512150G>T	NCBI36
NG_051023.1:g.1099353C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000389484.8:c.1789+10875C>A MANE Select	ENSP00000374135.3:n.1789+10875C>A
ENST00000389484.7:c.1789+10875C>A	ENSP00000374135.3:n.1789+10875C>A
ENST00000434794.1:c.206-55835C>A	ENSP00000413239.1:n.206-55835C>A
ENST00000618808.4:c.1447+10875C>A	ENSP00000478868.1:n.1447+10875C>A
NM_018557.2:c.1789+10875C>A	NP_061027.2:n.1789+10875C>A
XM_011511352.1:c.1900+10875C>A	XP_011509654.1:n.1900+10875C>A
XM_017004341.1:c.1399+10875C>A	XP_016859830.1:n.1399+10875C>A
XR_001738778.1:n.3523+10875C>A
NM_018557.3:c.1789+10875C>A MANE Select	NP_061027.2:n.1789+10875C>A